Methyl (2Z)-2-{[N-(2-formyl­phen­yl)-4-methyl­benzene­sulfonamido]­meth­yl}-3-(naphthalen-1-yl)prop-2-enoate

In the title compound, C29H25NO5S, the sulfonyl-bound benzene ring forms dihedral angles of 42.1 (1) and 48.5 (1)°, respectively, with the formyl-substituted benzene ring and the naphthalene residue. In the crystal, pairs of C—H⋯O inter­actions lead to the formation of R 2 2(10) inversion dimers, wh...

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Main Authors: Madhanraj, R., Murugavel, S., Kannan, D., Bakthadoss, M.
Format: Online
Language:English
Published: International Union of Crystallography 2012
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3275017/
id pubmed-3275017
recordtype oai_dc
spelling pubmed-32750172012-02-15 Methyl (2Z)-2-{[N-(2-formyl­phen­yl)-4-methyl­benzene­sulfonamido]­meth­yl}-3-(naphthalen-1-yl)prop-2-enoate Madhanraj, R. Murugavel, S. Kannan, D. Bakthadoss, M. Organic Papers In the title compound, C29H25NO5S, the sulfonyl-bound benzene ring forms dihedral angles of 42.1 (1) and 48.5 (1)°, respectively, with the formyl-substituted benzene ring and the naphthalene residue. In the crystal, pairs of C—H⋯O inter­actions lead to the formation of R 2 2(10) inversion dimers, which are linked by further C—H⋯O inter­actions into supra­molecular tapes running along [100]. The crystal packing is further stabilized by C—H⋯π inter­actions. International Union of Crystallography 2012-01-11 /pmc/articles/PMC3275017/ /pubmed/22346962 http://dx.doi.org/10.1107/S160053681200058X Text en © Madhanraj et al. 2012 http://creativecommons.org/licenses/by/2.0/uk/ This is an open-access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.
repository_type Open Access Journal
institution_category Foreign Institution
institution US National Center for Biotechnology Information
building NCBI PubMed
collection Online Access
language English
format Online
author Madhanraj, R.
Murugavel, S.
Kannan, D.
Bakthadoss, M.
spellingShingle Madhanraj, R.
Murugavel, S.
Kannan, D.
Bakthadoss, M.
Methyl (2Z)-2-{[N-(2-formyl­phen­yl)-4-methyl­benzene­sulfonamido]­meth­yl}-3-(naphthalen-1-yl)prop-2-enoate
author_facet Madhanraj, R.
Murugavel, S.
Kannan, D.
Bakthadoss, M.
author_sort Madhanraj, R.
title Methyl (2Z)-2-{[N-(2-formyl­phen­yl)-4-methyl­benzene­sulfonamido]­meth­yl}-3-(naphthalen-1-yl)prop-2-enoate
title_short Methyl (2Z)-2-{[N-(2-formyl­phen­yl)-4-methyl­benzene­sulfonamido]­meth­yl}-3-(naphthalen-1-yl)prop-2-enoate
title_full Methyl (2Z)-2-{[N-(2-formyl­phen­yl)-4-methyl­benzene­sulfonamido]­meth­yl}-3-(naphthalen-1-yl)prop-2-enoate
title_fullStr Methyl (2Z)-2-{[N-(2-formyl­phen­yl)-4-methyl­benzene­sulfonamido]­meth­yl}-3-(naphthalen-1-yl)prop-2-enoate
title_full_unstemmed Methyl (2Z)-2-{[N-(2-formyl­phen­yl)-4-methyl­benzene­sulfonamido]­meth­yl}-3-(naphthalen-1-yl)prop-2-enoate
title_sort methyl (2z)-2-{[n-(2-formyl­phen­yl)-4-methyl­benzene­sulfonamido]­meth­yl}-3-(naphthalen-1-yl)prop-2-enoate
description In the title compound, C29H25NO5S, the sulfonyl-bound benzene ring forms dihedral angles of 42.1 (1) and 48.5 (1)°, respectively, with the formyl-substituted benzene ring and the naphthalene residue. In the crystal, pairs of C—H⋯O inter­actions lead to the formation of R 2 2(10) inversion dimers, which are linked by further C—H⋯O inter­actions into supra­molecular tapes running along [100]. The crystal packing is further stabilized by C—H⋯π inter­actions.
publisher International Union of Crystallography
publishDate 2012
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3275017/
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